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(-)-Cannabidiol_Molecular_structure_CAS_13956-29-1)
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(-)-Cannabidiol

Catalog No. C175300 Name Toronto Research Chemicals
CAS Number 13956-29-1 Website http://www.trc-canada.com
M. F. C21H30O2 Telephone +1 (416) 665-9696
M. W. 314.4617 Fax +1 (416) 665-4439
Purity Email info@trc-canada.com
Storage -20°C Freezer, Under Inert Atmosphere Chembase ID: 163575

SYNONYMS

IUPAC name
2-[(6R)-3-methyl-6-(prop-1-en-2-yl)cyclohex-2-en-1-yl]-5-pentylbenzene-1,3-diol
IUPAC Traditional name
cannabidiol
Synonyms
CBD
(1R-trans)-2-[3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl-1,3-benzenediol
Δ1(2)-trans-Cannabidiol
2-[(1R,6R)-3-Methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-5-pentyl-1,3-benzenediol
(-)-CBD
trans-(-)-(2-p-Mentha-1,8-dien-3-yl-5-pentylresorcinol
(-)-trans-Cannabidiol

DATABASE IDS

CAS Number 13956-29-1

PROPERTIES

Certificate of Analysis Download
Apperance Off-White Solid
Melting Point 62-63°C
Solubility Chloroform
Solubility Methanol
MSDS Link Download
Storage Condition -20°C Freezer, Under Inert Atmosphere

DETAILS

Description (English)
Major non-psychoactive constituent of Cannabis. Exhibits multiple bioactivities including anticonvulsant, anxiolytic and anti-inflammatory effects. The (+)-isomers were more active than the (-)-isomers.

REFERENCES

  • Satoshi Yamaori et al.: Drug Metabolism
  • Mechoulam, R., et al.: J. Clin. Pharmacol., 42, 11S (2002)
  • Harvey, R., et al.: Science, 304, 884 (2002)
  • Haeseler, G., et al.: Br. J. Pharmacol., 145, 916 ( 2005), Betz, H., et al.: J. Neurochem., 97, 1600 (2002)